29
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Aging is associated with marked deficiency in circulating IGF‐1, which has been shown to contribute to age‐related cognitive decline. Impairment of moment‐to‐moment adjustment of cerebral blood flow ( CBF) via neurovascular coupling is thought to play a critical role in the genesis of age‐related cognitive impairment. To establish the link between IGF‐1 deficiency and cerebromicrovascular impairment, neurovascular coupling mechanisms were studied in a novel mouse model of IGF‐1 deficiency ( Igf1 f/f TBG‐Cre‐ AAV8) and accelerated vascular aging. We found that IGF‐1‐deficient mice exhibit neurovascular uncoupling and show a deficit in hippocampal‐dependent spatial memory test, mimicking the aging phenotype. IGF‐1 deficiency significantly impaired cerebromicrovascular endothelial function decreasing NO mediation of neurovascular coupling. IGF‐1 deficiency also impaired glutamate‐mediated CBF responses, likely due to dysregulation of astrocytic expression of metabotropic glutamate receptors and impairing mediation of CBF responses by eicosanoid gliotransmitters. Collectively, we demonstrate that IGF‐1 deficiency promotes cerebromicrovascular dysfunction and neurovascular uncoupling mimicking the aging phenotype, which are likely to contribute to cognitive impairment.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          Role of astrocytes in neurovascular coupling.

          Neural activity is intimately tied to blood flow in the brain. This coupling is specific enough in space and time that modern imaging methods use local hemodynamics as a measure of brain activity. In this review, we discuss recent evidence indicating that neuronal activity is coupled to local blood flow changes through an intermediary, the astrocyte. We highlight unresolved issues regarding the role of astrocytes and propose ways to address them using novel techniques. Our focus is on cellular level analysis in vivo, but we also relate mechanistic insights gained from ex vivo experiments to native tissue. We also review some strategies to harness advances in optical and genetic methods to study neurovascular coupling in the intact brain. Copyright © 2011 Elsevier Inc. All rights reserved.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Neuronal activity drives localized blood-brain-barrier transport of serum insulin-like growth factor-I into the CNS.

            Upon entry into the central nervous system (CNS), serum insulin-like growth factor-1 (IGF-I) modulates neuronal growth, survival, and excitability. Yet mechanisms that trigger IGF-I entry across the blood-brain barrier remain unclear. We show that neuronal activity elicited by electrical, sensory, or behavioral stimulation increases IGF-I input in activated regions. Entrance of serum IGF-I is triggered by diffusible messengers (i.e., ATP, arachidonic acid derivatives) released during neurovascular coupling. These messengers stimulate matrix metalloproteinase-9, leading to cleavage of the IGF binding protein-3 (IGFBP-3). Cleavage of IGFBP-3 allows the passage of serum IGF-I into the CNS through an interaction with the endothelial transporter lipoprotein related receptor 1. Activity-dependent entrance of serum IGF-I into the CNS may help to explain disparate observations such as proneurogenic effects of epilepsy, rehabilitatory effects of neural stimulation, and modulatory effects of blood flow on brain activity. 2010 Elsevier Inc. All rights reserved.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Impaired hippocampal-dependent learning and functional abnormalities in the hippocampus in mice lacking serotonin(1A) receptors.

              The hippocampus is a major limbic target of the brainstem serotonergic neurons that modulate fear, anxiety, and learning through postsynaptic serotonin(1A) receptors (5-HT(1A) receptors). Because chronic stress selectively down-regulates the 5-HT(1A) receptors in the hippocampus, we hypothesized that mice lacking these receptors may exhibit abnormalities reminiscent of symptoms of stress-related psychiatric disorders. In particular, a hippocampal deficit in the 5-HT(1A) receptor could contribute to the cognitive abnormalities often seen in these disorders. To test whether a deficit in 5-HT(1A) receptors impairs hippocampus-related functions, we studied hippocampal-dependent learning and memory, synaptic plasticity in the hippocampus, and limbic neuronal excitability in 5-HT(1A)-knockout (KO) mice. 5-HT(1A)-KO animals showed a deficit in hippocampal-dependent learning and memory tests, such as the hidden platform (spatial) version of the Morris water maze and the delayed version of the Y maze. The performance of KO mice was not impaired in nonhippocampal memory tasks such as the visible platform (nonspatial) version of the Morris water maze, the immediate version of the Y maze, and the spontaneous-alternation test of working memory. Furthermore, paired-pulse facilitation in the dentate gyrus of the hippocampus was impaired in 5-HT(1A)-KO mice. Finally, 5-HT(1A)-KO mice, as compared with wild-type animals, displayed higher limbic excitability manifested as lower seizure threshold and higher lethality in response to kainic acid administration. These results demonstrate that 5-HT(1A) receptors are required for maintaining normal hippocampal functions and implicate a role for the 5-HT(1A) receptor in hippocampal-related symptoms, such as cognitive disturbances, in stress-related disorders.
                Bookmark

                Author and article information

                Journal
                Aging Cell
                Aging Cell
                10.1111/(ISSN)1474-9726
                ACEL
                Aging Cell
                John Wiley and Sons Inc. (Hoboken )
                1474-9718
                1474-9726
                14 July 2015
                December 2015
                : 14
                : 6 ( doiID: 10.1111/acel.2015.14.issue-6 )
                : 1034-1044
                Affiliations
                [ 1 ] Donald W. Reynolds Department of Geriatric Medicine Reynolds Oklahoma Center on AgingUniversity of Oklahoma Health Sciences Center Oklahoma City OK 73104USA
                [ 2 ] Department of Neurosurgery and Szentagothai Research Center Medical SchoolUniversity of Pecs Pecs 7624Hungary
                [ 3 ] Department of PhysiologyUniversity of Oklahoma Health Sciences Center 940 S.L. Young Blvd. Rm. 653 Oklahoma City 73104 OKUSA
                [ 4 ] Division of Clinical PharmacologyVanderbilt University Medical Center D‐3100 Medical Center North Nashville TNUSA
                [ 5 ] Department of Medical Physics and Informatics Faculty of Medicine and Faculty of Science and InformaticsUniversity of Szeged Szeged 6720Hungary
                [ 6 ] The Peggy and Charles Stephenson Cancer CenterUniversity of Oklahoma Health Sciences Center Oklahoma City OK 73104USA
                [ 7 ] Department of Pulmonology1125 Budapest, Diós árok 1/c Semmelweis University BudapestHungary
                Author notes
                [*] [* ] Correspondence

                Zoltan Ungvari, MD, PhD; Anna Csiszar, MD, PhD, Department of Geriatric Medicine, Reynolds Oklahoma Center on Aging, University of Oklahoma HSC, 975 N. E. 10th Street ‐ BRC 1303, Oklahoma City, OK 73104, USA. Tel.: (405) 271‐7622; fax: 405‐271‐2298; e‐mails : zoltan-ungvari@ 123456ouhsc.edu ; anna-csiszar@ 123456ouhsc.edu

                [†]

                These authors contributed equally to this work.

                Article
                ACEL12372
                10.1111/acel.12372
                4693458
                26172407
                d096f280-5188-4f84-9cd6-9028bdc234cf
                © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 14 June 2015
                Page count
                Pages: 11
                Funding
                Funded by: American Heart Association
                Funded by: National Center for Complementary and Alternative Medicine
                Award ID: R01‐AT006526
                Funded by: National Institute on Aging
                Award ID: R01‐AG047879
                Award ID: R01‐AG038747
                Award ID: R01‐NS056218
                Funded by: Arkansas Claude Pepper Older Americans Independence Center at University of Arkansas Medical Center
                Award ID: P30 AG028718
                Funded by: Oklahoma Center for the Advancement of Science and Technology
                Funded by: Bolyai János Research Scholarship of the Hungarian Academy of Sciences
                Award ID: BO/00327/14/5
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                acel12372
                December 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.7.2 mode:remove_FC converted:22.12.2015

                Cell biology
                arachidonic acid metabolites,astrocyte,endothelial dysfunction,functional hyperemia,insulin‐like growth factor‐1,neurovascular uncoupling,nitric oxide,somatomedin c,vascular aging,vascular cognitive impairment

                Comments

                Comment on this article